Institut für Molekulare Mikrobiologie und Biotechnologie, Westfälische Wilhelms-Universität Münster, Corrensstrasse 3, 48149, Münster, Germany.
Appl Microbiol Biotechnol. 2013 Sep;97(17):7805-19. doi: 10.1007/s00253-013-4935-5. Epub 2013 May 5.
Bacillus pumilus mutants were generated by targeted deletion of a set of genes eventually facilitating genetic handling and assuring biological containment. The well-defined and stable mutants do not form functional endospores due to the deletion of yqfD, an essential sporulation gene; they are affected in DNA repair, as ΔuvrBA rendered them UV hypersensitive and, thus, biologically contained; they are deficient for the uracil phosphoribosyl-transferase (Δupp), allowing for 5-fluorouracil-based counterselection facilitating rapid allelic exchanges; and they are readily transformable due to the deletion of the restrictase encoding locus (ΔhsdR) of a type I restriction modification system. Vegetative growth as well as extracellular enzyme production and secretion are in no case affected. The combination of such gene deletions allows for development of B. pumilus strains suited for industrial use and further improvements.
通过靶向删除一组基因,生成了短小芽孢杆菌突变体,最终实现了遗传操作和生物控制。由于关键的孢子形成基因 yqfD 的缺失,这些明确且稳定的突变体无法形成功能性芽孢;它们在 DNA 修复方面受到影响,因为 ΔuvrBA 使它们对 UV 敏感,从而实现了生物控制;它们缺乏尿嘧啶磷酸核糖基转移酶(Δupp),这允许基于 5-氟尿嘧啶的反向选择,促进快速等位基因交换;并且由于 I 型限制修饰系统的限制酶编码基因座(ΔhsdR)的缺失,它们很容易转化。营养生长以及胞外酶的产生和分泌都没有受到影响。这样的基因缺失的组合使得能够开发适合工业用途的短小芽孢杆菌菌株,并进一步进行改进。